21 results on '"Campagna, Dean R."'
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2. Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice
3. Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency
4. A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia
5. Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9
6. A Novel Conditional Knockout of the Diamond Blackfan Anemia Gene Rpl11 Shows Failure of Erythropoiesis, a Marked Increase in BFU-E Progenitors By Phenotype That Proliferate Poorly in Culture, and Activation of p53 Target Genes
7. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)
8. Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in α-spectrin–deficient red cells
9. The Clinical and Genetic Spectrum of TMPRSS6 Mutations Leading to Inappropriate Hepcidin Expression and Iron Refractory Iron Deficiency Anemia (IRIDA).
10. Identification of a Steap3 endosomal targeting motif essential for normal iron metabolism
11. Systematic Analysis of Known Candidate Genes in 58 Probands with Previously Uncharacterized Congenital Sideroblastic Anemia: Evidence for Genetic Heterogeneity and Identification of Novel Mutations in ALAS2 and PUS1
12. Rsp1 Is Indispensable for mRNA Stability during Erythroid Terminal Differentiation
13. hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouse
14. Response: What's in a name?
15. X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation
16. Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis
17. The Steap proteins are metalloreductases
18. Identification and Characterization of an Erythrocyte Endosomal Ferrireductase Critical for Transferrin Dependent Iron Uptake.
19. X-Linked Gray Platelet Syndrome Due to a GATA1 Arg216Gln Mutation.
20. nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse
21. The molecular defect in hypotransferrinemic mice
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